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Intertumor heterogeneity in 60 pancreatic neuroendocrine tumors associated with multiple endocrine neoplasia type 1.

Andreas SelberheerOskar KoperekPhilipp RissChristian ScheubaMartin B NiederleReto KaderliAurel PerrenBruno Niederle
Published in: Orphanet journal of rare diseases (2019)
Tumor size of ≥20 mm seems to correlate with more aggressive MEN-1 related pancreatic disease, regardless of individual proliferation. Tumors ≥20 mm and tumors graded as G2 should be treated surgically regardless of their size.
Keyphrases
  • neuroendocrine tumors
  • high grade
  • signaling pathway
  • single cell
  • middle aged
  • newly diagnosed